Allele Registry

Canonical Allele Identifier: PA2830358182

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000049440

ClinVar Variation:

56031

HGVS (amino-acid)	Matching Registered Transcripts
NP_852111.2:p.Ala549Val	CA144121 NM_181446.3:c.1646C>T